Title
Hemodynamic and metabolic changes induced by cocaine in anesthetized rat observed with multimodal functional MRI
GSBS Program
Neuroscience
UMMS Affiliation
Department of Psychiatry, Center for Comparative Neuroimaging
Date
3-22-2006
Document Type
Article
Medical Subject Headings
Algorithms; Anesthesia; Animals; Blood Volume; Brain Chemistry; Cerebrovascular Circulation; Cocaine; Data Interpretation, Statistical; Hemodynamics; Hypercapnia; Injections, Intravenous; Magnetic Resonance Imaging; Male; Metabolism; Oxygen; Rats; Rats, Sprague-Dawley; Reward
Disciplines
Life Sciences | Medicine and Health Sciences | Neuroscience and Neurobiology
Abstract
RATIONALE: Physiological changes (such as heart rate and respiration rate) associated with strong pharmacological stimuli could change the blood-oxygenation-level-dependent (BOLD) functional magnetic resonance imaging (fMRI) mapping signals, independent of neural activity.
OBJECTIVES: This study investigates whether the physiological changes per se associated with systemic cocaine administration (1 mg/kg) contaminate the BOLD fMRI signals by measuring BOLD and cerebral blood flow (CBF) fMRI and estimating the cerebral metabolic rate of oxygen (CMRO(2)) changes.
MATERIALS AND METHODS: BOLD and CBF fMRI was performed, and changes in CMRO(2) were estimated using the BOLD biophysical model.
RESULTS: After systemic cocaine administration, blood pressure, heart rate, and respiration rate increased, fMRI signals remained elevated after physiological parameters had returned to baseline. Cocaine induced changes in the BOLD signal within regions of the reward pathway that were heterogeneous and ranged from -1.2 to 5.4%, and negative changes in BOLD were observed along the cortical surface. Changes in CBF and estimated CMRO(2) were heterogeneous and positive throughout the brain, ranging from 14 to 150% and 10 to 55%, respectively.
CONCLUSIONS: This study demonstrates a valuable tool to investigate the physiological and biophysical basis of drug action on the central nervous system, offering the means to distinguish the physiological from neural sources of the BOLD fMRI signal.
Rights and Permissions
Citation: Psychopharmacology (Berl). 2006 May;185(4):479-86. Epub 2006 Mar 21. Link to article on publisher's site